Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Keziban Bulan"'
Publikováno v:
Case Reports in Medicine, Vol 2014 (2014)
Hyperekplexia is a rare, nonepileptic, genetic, or sporadic neurologic disorder characterized by startle responses to acoustic, optic, or tactile stimuli. Genetic defects in glycine receptors as well as encephalitis, tumors, inflammation, and disgene
Externí odkaz:
https://doaj.org/article/112efb51eebc4c87bf9844b7a7c62448
Publikováno v:
Journal of Neonatal Surgery, Vol 3, Iss 1 (2014)
Though the perforation of the colon in neonates is rare, it is associated with more than 50% mortality in high-risk patients. We report a case of idiopathic neonatal perforation of the sigmoid colon in an 8-day-old, healthy, male neonate without any
Externí odkaz:
https://doaj.org/article/e2a1cb57cfaf4eda886593bea3529b10
Autor:
Keziban Bulan, Lokman Üstyol, Sultan Kaba, Nesrin Ceylan, Murat Doğan, Nihat Demir, Zeyneb Ümit Bozdoğan, Mehmet Deniz Bulut
Publikováno v:
Eastern Journal Of Medicine. 22:26-29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d84b82c96f90ec70a6333f93586c6766
https://doi.org/10.5505/ejm.2017.18480
https://doi.org/10.5505/ejm.2017.18480
Autor:
Keziban Bulan, Sekibe Zehra Dogan, Hatice Uce Özkol, Murat Doğan, Ahmet Koç, Nihat Demir, Sultan Kaba
Publikováno v:
Cutaneous and Ocular Toxicology. 33:70-73
The mucocutaneous changes observed during vitamin B12 deficiency in children have been published only as case studies and small case series. In this study, we aimed to demonstrate the frequency of mucocutaneous changes (particularly hyperpigmentation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6a5ad6ee636021b9a3c03f1a274971f
https://doi.org/10.3109/15569527.2013.861477
https://doi.org/10.3109/15569527.2013.861477
Background: This study was conducted to investigate CTNS (cystinosin, lysosomal cystine transporter) gene mutations and the clinical spectrum of nephropathic cystinosis among patients diagnosed with the disease in a single center in Turkey. Methods:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61b83b2f66f394850ff62183f50d764b
https://avesis.yyu.edu.tr/publication/details/51dae4f3-59fd-47fe-b45e-84ca8fd6938d/oai
https://avesis.yyu.edu.tr/publication/details/51dae4f3-59fd-47fe-b45e-84ca8fd6938d/oai
Publikováno v:
West Indian Medical Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a62e77e3ce4f4b86ea9317ed9f429bf2
https://doi.org/10.7727/wimj.2015.390
https://doi.org/10.7727/wimj.2015.390
Publikováno v:
The journal of maternal-fetalneonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 29(12)
Background: The purpose of this study was to evaluate whether or not platelet mass contributes to closure of patent ductus arteriosus (PDA) in premature newborns.Study design and subjects: This retrospective study included 115 preterm newborns with h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33b7eb31509f54b514883a3888f330c3
https://pubmed.ncbi.nlm.nih.gov/26169703
https://pubmed.ncbi.nlm.nih.gov/26169703
Autor:
Hüseyin Çaksen, Murat Doğan, Fatmagül Başarslan, Avni Kaya, Cahide Yilmaz, Keziban Bulan, Nebi Yılmaz, Sevil Arı Yuca
WOS: 000358581300007
PubMed: 24243939
In this study, lymphocyte subgroups including blood CD3, CD4, CD8, CD4/CD8, CD19, and CD16.56 values were analyzed in children with Down syndrome (DS). The study includes 85 children with DS, followed a
PubMed: 24243939
In this study, lymphocyte subgroups including blood CD3, CD4, CD8, CD4/CD8, CD19, and CD16.56 values were analyzed in children with Down syndrome (DS). The study includes 85 children with DS, followed a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::887420ed6ba0455f5fdd184d47143929
https://hdl.handle.net/20.500.12395/32130
https://hdl.handle.net/20.500.12395/32130
Publikováno v:
International Journal of Pediatric Otorhinolaryngology Extra. 8:50-52
Pierre Robin sequence (PRs) is a congenital disease characterized by micrognathia, cleft palate, glossoptosis and a wide range of other anomalies. The treatment of patients with PRs may be problematic due to the varying anomalies and high mortality r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a81e046bace595e082e196587bdacace
https://doi.org/10.1016/j.pedex.2013.02.003
https://doi.org/10.1016/j.pedex.2013.02.003